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利用适配体偶联的金纳米棒对稀有蛋白质进行富集和检测。

Enrichment and detection of rare proteins with aptamer-conjugated gold nanorods.

机构信息

Department of Chemistry, University of Florida, Gainesville, Florida 32611-7200, United States.

出版信息

Anal Chem. 2012 Jul 17;84(14):6008-15. doi: 10.1021/ac300806s. Epub 2012 Jun 25.


DOI:10.1021/ac300806s
PMID:22725611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3407574/
Abstract

Rare protein enrichment and sensitive detection hold great potential in biomedical studies and clinical practice. This work describes the use of aptamer-conjugated gold nanorods for the efficient enrichment of rare proteins from buffer solutions and human plasma. Gold nanorod (AuNR) surfaces were modified with a long PEG chain and a 15-mer thrombin aptamer for protein enrichment and detection. Studies of the effect of surface modification on enrichment efficiency of thrombin showed that a change of only one EG(6) linker unit, i.e., from 2EG(6) to 3EG(6), could increase thrombin protein capture efficiency by up to 47%. Furthermore, a 1 ppm sample of thrombin in buffer could be enriched with around 90% efficiency using a low concentration (0.19 nM) of gold nanorod probe modified with 3EG(6) spacer, and with the same probe, effective capture was achieved down to 10 ppb (1 ng) thrombin in plasma samples. In addition to α-thrombin enrichment, prothrombin was also efficiently captured from plasma samples via gold nanorods conjugated with 15-mer thrombin aptamer. Our work demonstrates efficient enrichment of rare proteins using aptamer-modified nanomaterials, which can be used in biomarker discovery studies.

摘要

稀有蛋白质的富集和敏感检测在生物医学研究和临床实践中具有巨大的潜力。本工作描述了使用适配体偶联的金纳米棒从缓冲溶液和人血浆中高效富集稀有蛋白质的方法。金纳米棒(AuNR)表面通过长 PEG 链和 15 个碱基的凝血酶适配体进行修饰,用于蛋白质的富集和检测。研究表面修饰对凝血酶富集效率的影响表明,仅仅改变一个 EG(6)连接单元,即从 2EG(6)变为 3EG(6),就可以将凝血酶蛋白的捕获效率提高多达 47%。此外,使用修饰有 3EG(6)间隔物的低浓度(0.19 nM)金纳米棒探针,可将缓冲液中 1 ppm 的凝血酶样品高效富集 90%左右,而使用相同的探针,可在血浆样品中有效捕获低至 10 ppb(1 ng)的凝血酶。除了α-凝血酶的富集外,通过与 15 个碱基的凝血酶适配体偶联的金纳米棒,也可以从血浆样品中有效捕获凝血酶原。我们的工作证明了使用适配体修饰的纳米材料可以有效地富集稀有蛋白质,这可用于生物标志物发现研究。

相似文献

[1]
Enrichment and detection of rare proteins with aptamer-conjugated gold nanorods.

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[2]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Self-assembly of phospholipid-PEG coating on nanoparticles through dual solvent exchange.

Nano Lett. 2011-8-1

[2]
Competitive protection of aptamer-functionalized gold nanoparticles by controlling the DNA assembly.

Anal Chem. 2011-7-28

[3]
Nanoparticle PEGylation for imaging and therapy.

Nanomedicine (Lond). 2011-6

[4]
The design and application of fluorophore-gold nanoparticle activatable probes.

Phys Chem Chem Phys. 2011-3-7

[5]
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Angew Chem Int Ed Engl. 2011-1-27

[6]
A dual platform for selective analyte enrichment and ionization in mass spectrometry using aptamer-conjugated graphene oxide.

J Am Chem Soc. 2010-11-22

[7]
Longitudinal surface plasmon resonance based gold nanorod biosensors for mass spectrometry.

Langmuir. 2010-4-20

[8]
HD1, a thrombin- and prothrombin-binding DNA aptamer, inhibits thrombin generation by attenuating prothrombin activation and thrombin feedback reactions.

Thromb Haemost. 2009-9-15

[9]
Sensitive plasma protein analysis by microparticle-based proximity ligation assays.

Mol Cell Proteomics. 2009-11-27

[10]
Quantitative nanoproteomics for protein complexes (QNanoPX) related to estrogen transcriptional action.

Mol Cell Proteomics. 2009-10-5

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